caffeine citrate
Generic: caffeine citrate
Labeler: sun pharmaceutical industries, inc.Drug Facts
Product Profile
Brand Name
caffeine citrate
Generic Name
caffeine citrate
Labeler
sun pharmaceutical industries, inc.
Dosage Form
INJECTION
Routes
Active Ingredients
caffeine citrate 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
47335-289
Product ID
47335-289_f32e4ba0-3e6d-41b3-95f3-67b040cd4529
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090077
Listing Expiration
2026-12-31
Marketing Start
2014-06-05
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
47335289
Hyphenated Format
47335-289
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
caffeine citrate (source: ndc)
Generic Name
caffeine citrate (source: ndc)
Application Number
ANDA090077 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (47335-289-27) / 3 mL in 1 VIAL, SINGLE-DOSE (47335-289-26)
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "f32e4ba0-3e6d-41b3-95f3-67b040cd4529", "openfda": {"upc": ["0347335290448"], "unii": ["U26EO4675Q"], "rxcui": ["849928", "849931"], "spl_set_id": ["d06d3810-9923-4199-be5e-ee5ee086b0a4"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (47335-289-27) / 3 mL in 1 VIAL, SINGLE-DOSE (47335-289-26)", "package_ndc": "47335-289-27", "marketing_start_date": "20140605"}], "brand_name": "Caffeine Citrate", "product_id": "47335-289_f32e4ba0-3e6d-41b3-95f3-67b040cd4529", "dosage_form": "INJECTION", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]", "Methylxanthine [EPC]", "Xanthines [CS]"], "product_ndc": "47335-289", "generic_name": "Caffeine Citrate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Caffeine Citrate", "active_ingredients": [{"name": "CAFFEINE CITRATE", "strength": "20 mg/mL"}], "application_number": "ANDA090077", "marketing_category": "ANDA", "marketing_start_date": "20140605", "listing_expiration_date": "20261231"}